ClubSub-P: Cluster-Based Subcellular Localization Prediction for Gram-Negative Bacteria and Archaea

Tekijä Paramasivam, Nagarajan, Linke, Dirk
Julkaistu 2011

Is the C-terminal insertional signal in Gram-negative bacterial outer membrane proteins species-specific or not?

Tekijä Paramasivam, Nagarajan, Habeck, Michael, Linke, Dirk
Julkaistu 2012

Pedigree based DNA sequencing pipeline for germline genomes of cancer families

Tekijä Försti, Asta, Kumar, Abhishek, Paramasivam, Nagarajan, Schlesner, Matthias, Catalano, Calogerina, Dymerska, Dagmara, Lubinski, Jan, Eils, Roland, Hemminki, Kari
Julkaisussa Hered Cancer Clin Pract (2016)

SIPA1L3 identified by linkage analysis and whole-exome sequencing as a novel gene for autosomal recessive congenital cataract

Tekijä Evers, Christina, Paramasivam, Nagarajan, Hinderhofer, Katrin, Fischer, Christine, Granzow, Martin, Schmidt-Bacher, Annette, Eils, Roland, Steinbeisser, Herbert, Schlesner, Matthias, Moog, Ute
Julkaisussa Eur J Hum Genet (2015)

Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family

Tekijä Kumar, Abhishek, Bandapalli, Obul Reddy, Paramasivam, Nagarajan, Giangiobbe, Sara, Diquigiovanni, Chiara, Bonora, Elena, Eils, Roland, Schlesner, Matthias, Hemminki, Kari, Försti, Asta
Julkaisussa Sci Rep (2018)

A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer

Tekijä Srivastava, Aayushi, Miao, Beiping, Skopelitou, Diamanto, Kumar, Varun, Kumar, Abhishek, Paramasivam, Nagarajan, Bonora, Elena, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Julkaisussa Cancers (Basel) (2020)

Whole Genome Sequencing Prioritizes CHEK2, EWSR1, and TIAM1 as Possible Predisposition Genes for Familial Non-Medullary Thyroid Cancer

Tekijä Srivastava, Aayushi, Giangiobbe, Sara, Skopelitou, Diamanto, Miao, Beiping, Paramasivam, Nagarajan, Diquigiovanni, Chiara, Bonora, Elena, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Julkaisussa Front Endocrinol (Lausanne) (2021)

Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing

Tekijä Srivastava, Aayushi, Giangiobbe, Sara, Kumar, Abhishek, Paramasivam, Nagarajan, Dymerska, Dagmara, Behnisch, Wolfgang, Witzens-Harig, Mathias, Lubinski, Jan, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Julkaisussa Front Bioeng Biotechnol (2020)

Cancer Predisposition Genes in Cancer-Free Families

Tekijä Zheng, Guoqiao, Catalano, Calogerina, Bandapalli, Obul Reddy, Paramasivam, Nagarajan, Chattopadhyay, Subhayan, Schlesner, Matthias, Sijmons, Rolf, Hemminki, Akseli, Dymerska, Dagmara, Lubinski, Jan, Hemminki, Kari, Försti, Asta
Julkaisussa Cancers (Basel) (2020)

A rare large duplication of MLH1 identified in Lynch syndrome

Tekijä Kumar, Abhishek, Paramasivam, Nagarajan, Bandapalli, Obul Reddy, Schlesner, Matthias, Chen, Tianhui, Sijmons, Rolf, Dymerska, Dagmara, Golebiewska, Katarzyna, Kuswik, Magdalena, Lubinski, Jan, Hemminki, Kari, Försti, Asta
Julkaisussa Hered Cancer Clin Pract (2021)

Whole Exome Sequencing Identifies APCDD1 and HDAC5 Genes as Potentially Cancer Predisposing in Familial Colorectal Cancer

Tekijä Skopelitou, Diamanto, Miao, Beiping, Srivastava, Aayushi, Kumar, Abhishek, Kuswick, Magdalena, Dymerska, Dagmara, Paramasivam, Nagarajan, Schlesner, Matthias, Lubinski, Jan, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Julkaisussa Int J Mol Sci (2021)

A Novel Low-Risk Germline Variant in the SH2 Domain of the SRC Gene Affects Multiple Pathways in Familial Colorectal Cancer

Tekijä Skopelitou, Diamanto, Miao, Beiping, Srivastava, Aayushi, Kumar, Abhishek, Kuświk, Magdalena, Dymerska, Dagmara, Paramasivam, Nagarajan, Schlesner, Matthias, Lubiński, Jan, Hemminki, Kari, Försti, Asta, Bandapalli, Obul Reddy
Julkaisussa J Pers Med (2021)

The Frog Xenopus as a Model to Study Joubert Syndrome: The Case of a Human Patient With Compound Heterozygous Variants in PIBF1

Tekijä Ott, Tim, Kaufmann, Lilian, Granzow, Martin, Hinderhofer, Katrin, Bartram, Claus R., Theiß, Susanne, Seitz, Angelika, Paramasivam, Nagarajan, Schulz, Angela, Moog, Ute, Blum, Martin, Evers, Christina M.
Julkaisussa Front Physiol (2019)

Evidence That Non-Syndromic Familial Tall Stature Has an Oligogenic Origin Including Ciliary Genes

Tekijä Weiss, Birgit, Eberle, Birgit, Roeth, Ralph, de Bruin, Christiaan, Lui, Julian C., Paramasivam, Nagarajan, Hinderhofer, Katrin, van Duyvenvoorde, Hermine A., Baron, Jeffrey, Wit, Jan M., Rappold, Gudrun A.
Julkaisussa Front Endocrinol (Lausanne) (2021)

Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic Cancer

Tekijä Slater, Emily P., Wilke, Lisa M., Böhm, Lutz Benedikt, Strauch, Konstantin, Lutz, Manuel, Gercke, Norman, Matthäi, Elvira, Hemminki, Kari, Försti, Asta, Schlesner, Matthias, Paramasivam, Nagarajan, Bartsch, Detlef K.
Julkaisussa J Pers Med (2021)

Segregation and potential functional impact of a rare stop-gain PABPC4L variant in familial atypical Parkinsonism

Tekijä Aslam, Muhammad, Ullah, Anwar, Paramasivam, Nagarajan, Kandasamy, Nirosiya, Naureen, Saima, Badshah, Mazhar, Khan, Kafaitullah, Wajid, Muhammad, Abbasi, Rashda, Eils, Roland, Brockmann, Marc A., Schlesner, Matthias, Ahmad, Nafees, von Engelhardt, Jakob
Julkaisussa Sci Rep (2019)

TALEN/CRISPR-mediated engineering of a promoterless anti-viral RNAi hairpin into an endogenous miRNA locus

Tekijä Senís, Elena, Mockenhaupt, Stefan, Rupp, Daniel, Bauer, Tobias, Paramasivam, Nagarajan, Knapp, Bettina, Gronych, Jan, Grosse, Stefanie, Windisch, Marc P., Schmidt, Florian, Theis, Fabian J., Eils, Roland, Lichter, Peter, Schlesner, Matthias, Bartenschlager, Ralf, Grimm, Dirk
Julkaisussa Nucleic Acids Res (2017)

A novel homozygous ARL13B variant in patients with Joubert syndrome impairs its guanine nucleotide-exchange factor activity

Tekijä Rafiullah, Rafiullah, Long, Alyssa B., Ivanova, Anna A., Ali, Hazrat, Berkel, Simone, Mustafa, Ghulam, Paramasivam, Nagarajan, Schlesner, Matthias, Wiemann, Stefan, Wade, Rebecca C., Bolthauser, Eugen, Blum, Martin, Kahn, Richard A., Caspary, Tamara, Rappold, Gudrun A.
Julkaisussa Eur J Hum Genet (2017)

Putative second hit rare genetic variants in families with seemingly GBA-associated Parkinson’s disease

Tekijä Aslam, Muhammad, Kandasamy, Nirosiya, Ullah, Anwar, Paramasivam, Nagarajan, Öztürk, Mehmet Ali, Naureen, Saima, Arshad, Abida, Badshah, Mazhar, Khan, Kafaitullah, Wajid, Muhammad, Abbasi, Rashda, Ilyas, Muhammad, Eils, Roland, Schlesner, Matthias, Wade, Rebecca C., Ahmad, Nafees, von Engelhardt, Jakob
Julkaisussa NPJ Genom Med (2021)

Characterization of rare germline variants in familial multiple myeloma

Tekijä Catalano, Calogerina, Paramasivam, Nagarajan, Blocka, Joanna, Giangiobbe, Sara, Huhn, Stefanie, Schlesner, Matthias, Weinhold, Niels, Sijmons, Rolf, de Jong, Mirjam, Langer, Christian, Preuss, Klaus-Dieter, Nilsson, Björn, Durie, Brian, Goldschmidt, Hartmut, Bandapalli, Obul Reddy, Hemminki, Kari, Försti, Asta
Julkaisussa Blood Cancer J (2021)